Method and apparatus for establishing additive differential on surfaces for preferential plating
A method and apparatus for establishing additive differential on surfaces for preferential plating of conductive material on the surface of a semiconductor wafer having surface portions and cavities on the surface. An additive is adsorbed on the surface in an auxiliary chamber. Conductive material is electrodeposited on the surface after the wafer is transported from the auxiliary chamber to the plating chamber. A sweeper is used to establish a differential in an adsorbed concentration of the additive between the surface portion and the cavities. The differential affects the rate of deposition of the conductive material.
This application is a CIP continuation-in-part of U.S. patent application Ser. No. 10/358,925, filed Feb. 4, 2003 (attorney docket No. ASMNUT.081DV1, ASM Ref. No. NT-020D), which is a divisional of U.S. Pat. No. 6,534,116 (ASM Ref. No. NT-020), filed Dec. 18, 2000 as U.S. patent application Ser. No. 09/740,701.
FIELD OF THE INVENTIONThe present invention relates generally to a semiconductor plating method and apparatus. More particularly, the present invention is directed to a method and apparatus that creates a differential between additive adsorbed on a first portion of a workpiece and additive adsorbed on a second portion of the workpiece using an external influence to enhance plating of a conductive material in the second portion of the workpiece.
BACKGROUND OF THE INVENTIONThere are many steps required in manufacturing multi-level integrated circuits (IC). Such steps include depositing conductive and insulator materials on a semiconductor wafer or substrate, followed by full or partial removal of these materials using photo-resist patterning, etching, and the like. After photolithography, patterning and etching steps, the resulting surface is generally non-planar as it contains many cavities or features, such as vias, lines, trenches, channels, bond-pads, and the like that come in a wide variety of dimensions and shapes. These features are typically filled with a highly conductive metal material before additional processing steps, such as etching and/or chemical mechanical polishing (CMP) is/are performed. Accordingly, a low resistance interconnection structure is formed between the various levels/sections of the IC.
Copper (Cu) is quickly becoming the preferred material for interconnections in ICs because of its low electrical resistivity and high resistance to electro-migration. Electrodeposition is one of the most popular methods for depositing Cu into the features on the substrate surface.
As can be expected, there are many different designs of Cu plating systems that have been used in this industry. For example, U.S. Pat. No. 5,516,412, issued on May 14, 1996 to Andricacos et al., discloses a vertical paddle plating cell that is designed to electrodeposit a film on a flat article. Next, U.S. Pat. No. 5,985,123, issued on Nov. 16, 1999 to Koon, discloses yet another vertical electroplating apparatus, which purports to overcome the non-uniform deposition problems associated with varying substrate sizes. Further, U.S. Pat. No. 5,853,559, issued on Dec. 29, 1998 to Tamaki et al., discloses an electroplating apparatus that minimizes waste of the plating electrolyte and accomplishes high recovery of the electrolyte.
During the Cu electrodeposition process, specially formulated plating solutions or electrolyte are used. These solutions or electrolyte contain ionic species of Cu and additives to control the texture, morphology, and the plating behavior of the deposited material. Additives are needed to make the deposited layers smooth and somewhat shiny.
There are many types of Cu plating solution formulations, some of which are commercially available. One such formulation includes Cu-sulfate (CUSO4) as the copper source (see James Kelly et al., Journal of The Electrochemical Society, Vol. 146, pages 2540-2545, (1999)) and includes water, sulfuric acid (H2SO4), and a small amount of chloride ions. As is well known, other chemicals can be added to the Cu plating solution to achieve desired properties of the deposited material.
The additives in the Cu plating solution can be classified under several categories, such as suppressors, levelers, brighteners, grain refiners, wetting agents, stress-reducing agents, accelerators, etc. In many instances, different classifications are often used to describe similar functions of these additives. Today, solutions used in electronic applications, particularly in manufacturing ICs, contain simpler additives consisting of two-component, two-ingredient packages (e.g., see Robert Mikkola and Linlin Chen, “Investigation of the Roles of the Additive Components for Second Generation Copper Electroplating Chemistries used for Advanced Interconnect Metallization”, Proceedings of the International Interconnect Technology Conference, pages 117-119, Jun. 5-7, 2000). These formulations are generically known as suppressors and accelerators.
Suppressors are typically polymers formulated from polyethylene glycol-PEG or polypropylene glycol-PPG and are believed to attach themselves to the substrate surface at high current density regions, thereby forming a high resistance film and suppressing the material deposited thereon. Accelerators are typically organic disulfides that enhance Cu deposition on portions of the substrate surface where they are adsorbed. The interplay between these two additives, and possibly the chloride ions, determines the nature of the Cu deposit.
The following figures are used to more fully describe the conventional electrodeposition method and apparatus.
In
The Cu material 7 completely fills the via 4a and is generally uniform in the large trench 4b, but does not completely fill the trench 4b because the additives that are used are not operative in large features. For example, it is believed that the bottom-up deposition into the via 4a occurs because the suppressor/inhibitor molecules attach themselves to the top of the via 4a to suppress the material growth thereabouts. These molecules cannot effectively diffuse to the bottom surface of the via 4a through the narrow opening. Preferential adsorption of the accelerator on the bottom surface of the via 4a results in faster growth in that region, resulting in bottom-up growth and the Cu deposit profile, shown in
Adsorption characteristics of the suppressor and accelerator additives on the bottom surface of the large trench 4b are not expected to be any different than the adsorption characteristics on the top surface of the field regions 8 of the substrate. Therefore, the Cu thickness t1 at the bottom surface of the trench 4b is about the same as the Cu thickness t2 over the field regions 8.
As can be expected, to completely fill the trench 4b with the Cu material 7, further plating is required.
Thus far, much attention has been focused on the development of Cu plating chemistries and plating techniques that yield bottom-up filling of small features on substrates. This is desirable because, as mentioned above, lack of bottom-up filling can cause defects in the small features. As part of these development efforts, it was discovered that the filling behavior of the small features could be affected not only by the solution chemistry, but also by the type of the power supply used for electrodeposition.
Recent studies suggest that it might be preferable to use pulse or pulse-reverse plating methods to deposit defect free Cu into the small vias (e.g., U.S. Pat. No. 5,972,192, issued to Dubin et al. on Oct. 26, 1999, and Gandikota et al. “Extension of Copper Plating to 0.13 um Nodes by Pulse-Modulated Plating”, Proceedings of the International Interconnect Technology Conference, pages 239-241, Jun. 5-7, 2000). In the pulse-reverse plating process, a cathodic voltage pulse rather than a cathodic DC voltage is applied to the substrate surface. After a short period of plating during the cathodic pulse, the polarity of the voltage is reversed for a brief period causing electrochemical etching from the deposited material. Plating and etching cycles are then repeated until the small features are filled with high quality Cu. A recent study (e.g., C. H. Hsieh et al., “Film Properties and Surface Profile after Gap Fill of Electrochemically Deposited Cu Films by DC and Pulse Reverse Processes”, Proceedings of the International Interconnect Technology Conference, pages 182-184, Jun. 5-7, 2000), shows that the filling of the vias is controlled mainly by the additive diffusion when the DC process is used, whereas it is mainly controlled by additive adsorption when a pulse-reverse process is used.
As described above, the attention in the semiconductor industry has mainly been concentrated on filling the various features on semiconductor wafers with Cu. Both DC and pulsed power supplies have been used in the deposition of these Cu films. Filling properties of Cu into small features was found to be a strong function of the type of the power supply used. Although the exact roles of the plating solution additives and their interaction with the applied voltage waveforms are not well understood, it is clear that the kinetics of the additive adsorption and diffusion processes influence the way metals deposit on non-planar substrate surfaces.
As mentioned above, special bath formulations and pulse plating processes have been developed to obtain bottom-up filling of the small features. However, these techniques have not been found effective in filling the large features. In large features, the additives can freely diffuse in and out of them. The use of standard pulse plating techniques, in conjunction with the commonly used additive systems containing chloride ions, accelerators and suppressors/inhibitors, does not yield accelerated growth from the bottom surface of the features where the width of the feature is considerably larger than its depth. The growth of Cu in such features is conformal and the film thickness deposited on the bottom surface of the large features is approximately the same as that deposited on the field regions.
Methods and apparatuses to achieve accelerated bottom-up plating in small as well as large features on a substrate would be invaluable in terms of process efficiency and cost since such a process would yield a Cu deposit that is generally planar, as illustrated in
Others have previously recognized attractive features of a plated Cu structure, such as the one shown in
In the U.S. Pat. No. 6,176,992, entitled “Method and apparatus for electrochemical mechanical deposition”, commonly owned by the assignee of the present invention and hereby incorporated by reference in its entirety, a technique is disclosed that achieves deposition of the conductive material into the cavities on the substrate surface while minimizing deposition on the field regions by polishing the field regions with a pad as the conductive material is deposited. The plating electrolyte in this application is supplied to the small gap between the pad and the substrate surface through a porous pad or through asperities in the pad.
The anode assembly 19 can also be rotated around a second axis 10c at controlled speeds in both the clockwise and counter-clockwise directions. It is also to be understood that axes 10b and 10c are substantially parallel to each other. The gap between the wafer 16 and the pad 18 is adjustable by moving the carrier head 10 in the z direction. When the wafer 16 surface and the pad 18 are in contact, the pressure that is exerted on the two surfaces can also be adjusted. The U.S. Pat. No. 6,413,388, entitled “Pad Designs and Structures for a Versatile Materials Processing Apparatus”, filed Feb. 23, 2000, describes various shapes and forms of the holes in the pad, through which the electrolyte flows to the wafer surface.
During operation, a potential is applied between the electrical lead 17 to the wafer 16 and the electrical lead 24 to the anode assembly 19, making the wafer 16 surface more negative than the anode assembly 19. The electrolyte 20 can be introduced to the pad 18 from a reservoir (not shown) located in proximity to the anode assembly 19. The anode assembly 19 can have an in-channel and holes that are made therein, which together provide a path for the electrolyte 20 to be fed to the gap between the pad 18 and the wafer 16.
Under applied potential, Cu plates out of the electrolyte 20 onto the wafer 16 surface. The moving pad 18 that is pushed against the wafer 16 surface at a controlled pressure minimizes accumulation of Cu over certain portions of the wafer 16 surface by polishing the same.
The pad 18 is preferably made of nonconductive, hard, porous, or perforated type material so that an electric field can pass through it, while preventing shorting between the anode assembly 19 and the cathode wafer 16. The spacing or gap between the pad 18 and the cathode wafer 16 may range from less than 1 micron up to 2 millimeters. The diameter or cross-sectional length of the pad 18 and the wafer 16 may range from about 5 millimeters to over 300 millimeters. The larger the wafer 16 diameter, the larger the pad 18 diameter.
SUMMARYIn accordance with an aspect of the invention, a system is provided for electrodepositing a conductive material onto a surface of a wafer. The surface includes a surface portion and a cavity portion. The system includes an auxiliary chamber and a plating chamber. The auxiliary chamber is configured for having an additive adsorbed on the upper surface portion and the cavity portion of the surface. The plating chamber is configured to electrodeposit the conductive material to form a conductive layer on the surface.
In accordance with another aspect of the invention, a system is provided for electrodepositing a conductive material onto a surface of a wafer. The surface includes an upper surface portion and a cavity portion. The system includes a first chamber and a second chamber. The first chamber includes additive applying means for having an additive adsorbed on the upper surface portion and the cavity portion of the surface. The second chamber includes a plating means for electrodepositing the conductive material on the surface.
In accordance with yet another aspect of the invention, a method is provided for electrodepositing a conductive material onto a surface of a wafer. The surface includes an upper surface portion and a cavity portion. An additive is adsorbed on the upper surface portion and the cavity portion of the surface in a first chamber. The wafer is transported to a second chamber after adsorbing. The conductive material is electrodeposited to form a conductive layer on the surface in the second chamber.
BRIEF DESCRIPTION OF THE DRAWINGSThese and other objects and advantages of the present invention will become apparent and more readily appreciated from the following detailed description of the presently preferred exemplary embodiments of the invention taken in conjunction with the accompanying drawings, of which:
Preferred embodiments will be described herein with reference to the following figures. By mask-pulsed plating the conductive material on the substrate surface, a more desirable and high quality conductive material can be deposited in the various features therein.
Embodiments described herein can be used with any substrate, such as a semiconductor wafer, flat panel, magnetic film head, packaging substrate, and the like. Further, specific processing parameters, such as time, pressure, mask designs, and the like, are provided herein, which specific parameters are intended to be explanatory rather than limiting.
The plating method described herein is called “mask-pulsed” plating. The embodiments discussed herein describe a method and apparatus for mask-pulse plating conductive material onto a substrate by intermittently moving a mask to make contact with the substrate surface and applying power between an anode and the substrate, the mask being positioned in between the anode and the substrate. Furthermore, embodiments are directed to novel plating methods and apparatuses that provide enhanced electrodeposition of conductive materials into the various features on the substrate surface.
In
Referring back to
As can be seen from the above example, a DC power supply can be used for this plating technique. By moving the solid insulating mask 40 that makes physical contact with the wafer 32, any section on the wafer surface can be suddenly and briefly exposed to the electrolyte and to the applied plating current. This is quite different from the prior art techniques defined above. For instance, in embodiments described herein, certain sections of the wafer surface are substantially free from the electrolyte. The electrolyte is applied to a section of the wafer when that section is exposed to the electrolyte and a pulse of current is simultaneously applied.
If the current mask-pulsed plating method is used with simple metal deposition electrolytes with no additives (i.e., inhibitors and accelerators), it would not be expected to be much different than conventional plating. This is because the size of the openings 42 in the mask 40 is typically much larger than the feature size on the wafer 32 surface. Therefore, when a section is exposed through the opening 42 to the electrolyte, regular plating would commence. However, if additives are added that influence polarization, then the mask-pulsed plating method can offer advantages that are not existent in conventional pulsed plating techniques.
For example, consider a Cu plating bath containing conventional solutions/chemicals (e.g., Cu sulfate, water, sulfuric acid and chloride ions) and an additive A. The additive A enhances deposition when it is adsorbed on the wafer surface. When this electrolyte is used in a conventional plating cell, such as the one depicted in
If, however, the mask-pulsed plating technique is used with the same electrolyte, the mask would clear away at least a portion of the additive A from the upper supprt portions or field regions since it makes physical contact with these regions. Both the small and large features, however, will still contain the adsorbed additive A since these features are not in direct physical contact with the mask. When a section of the wafer is suddenly exposed to the electrolyte, the bottom and side surfaces of the features (cavity portions) with the previously adsorbed additive A would immediately start plating at a higher rate than the field regions. If the time period Δt is less than the adsorption period required for the additive A to attach itself to the substrate surface, the applied plating current preferentially flows through the features to be filled, thereby yielding an enhanced deposition rate within the features in relation to the deposition rate on the field regions.
The mask-pulsed plating method described herein utilizes the differences between response times of various additives to achieve enhanced plating into the various features of the substrate surface. The mechanism involves “sweeping” of the top surface of the substrate (field regions) by the mask, which does not make physical contact with the regions inside the features. The sweeping on the field regions establishes a differential between the concentration of the adsorbed species in those regions that are swept away and the regions that are within the features. When the surface is then suddenly exposed to the electrolyte and the electric field, the features with the adsorbed species attracts most of the plating current from the field regions.
This method works equally well using multiple additives. For example, if the plating solution contains an inhibitor B and an accelerator C with the adsorption kinetics of the inhibitor being much faster than that of accelerator, the following mechanism can be used by the mask-pulsed plating method. Both the inhibitor B and the accelerator C would be partially or wholly swept off the field regions of the substrate by the mask. However, both species would still be present in the cavities or features. When the substrate is exposed to the electrolyte and the electric field, the inhibitor B would readily adsorb onto the upper surface portions or field regions, introducing a high resistance path for the plating current. The accelerator C, which is already present within the features, compensates for the action of the inhibitor in those regions and the current can easily flow through these features. Therefore, until the accelerator C is properly adsorbed onto the field regions, the film growth rate within the features will be higher.
This same result can also be expected from yet another chemistry where an inhibitor D has the property of strong adsorption and an accelerator E is weakly bonded to the field regions. In this case, the mask can readily remove the weakly bonded accelerator E from the field regions whereas, the accelerator E remains attached to the surfaces within the features. Upon exposure to the electrolyte and electric field, the plating current flows through the features preferentially until the accelerator E begins to get adsorbed again onto the field regions.
It should be noted that the above descriptions are just some examples of the mechanisms involved in the embodiments described herein and are not meant to be limiting. The embodiments described herein utilize differences between adsorption/de-sorption kinetics of various electrolyte additives. The embodiments described herein accomplish this by applying a solution and power suddenly and simultaneously to a specific section of the substrate surface that has been previously cleared off, partially or wholly, of one or more of the additive species.
In the following section, an exemplary process sequence using a system 100 will be described with reference to
Referring to
Once the additives are adsorbed on the surface 101, as shown in
As shown in
If the additive adsorbed on the surface in the auxiliary chamber (see
As described above, deposition is enhanced into the feature 202 as soon as the surface 200 is exposed to the plating electrolyte right after sweeping (
As for the accelerators that are swept off the upper surface portion or surface region 204 during sweeping by the mask or sweeper 118, they become included into the plating electrolyte. Therefore, even if their molecular structure may be different, accelerators could, in principal, come back and re-adsorb onto the upper surface portion or surface region 204 if their adsorption kinetics were as fast as or faster than that of suppressors. But as long as the suppressor concentration of the electrolyte is much larger than the concentration of accelerators introduced from the wafer surface due to sweeping, adsorption is dominated by the suppressors. This is because adsorption of additives from a solution onto a surface is also a function of their respective concentrations in the solution, with higher concentrations giving rise to higher adsorption on the surface. The exemplary plating solution discussed here may contain 1-10000 micromoles of suppressors, such as PEG, whereas the accelerator concentration introduced into the bath due to surface sweeping may be much smaller than 1 micromole. These calculations may be readily made, depending upon the nature and chemistry of the specific accelerator and suppressor additives used in the process, and the suppressor concentration in the plating solution may be adjusted accordingly to assure a much higher suppressor concentration in the plating electrolyte than the swept off accelerator concentration.
As described above and shown in
After completing the electroplating process, the wafer W held by the wafer carrier 120 is preferably retracted into the auxiliary chamber 102, shown in
The geometry of the plating system shown in
-
- 1. The mask and the wafer surface should be engaged well when in contact. The mask surface facing the wafer may contain abrasives to help “sweep” away the additives more efficiently.
- 2. There should be a relative movement between the wafer and the mask. The wafer, mask, or both may be moved in linear or orbital manner or combination thereof.
- 3. There should be substantially no electrolyte between the mask and the wafer surface, i.e., physical contact between the wafer surface and the mask surface should be good. The wafer surface should be exposed to electrolyte through the opening(s) in the mask.
- 4. The size of the opening(s) in the mask and the speed of the relative motion between the mask and the wafer should be such that any section on the wafer should be exposed to the electrolyte only briefly, typically for less than two seconds, preferably less than one second, e.g., 10-500 msec. This time interval should be adjusted with respect to the adsorption characteristics of the additives being used.
The power supply used in these embodiments may be pulsed or a DC power supply, but preferably it is a DC power supply. The power supply can be used in the current controlled or voltage controlled mode, i.e., it either keeps the applied current constant or applied voltage constant. For the case of using a current controlled mode, it is important that the size of the opening(s) in the mask be large enough to cover portions of the field regions as well as portions of the features simultaneously. In other words, when the wafer surface is exposed to the electrolyte through the opening(s), there should not be just the field regions that are exposed to the electrolyte at any given time. For example, if the opening is very small or the number of features on the wafer surface is low (low density features), the field regions are exposed to the electrolyte. In this case, since the power supply pushes through a fixed current, all the current would flow through the field regions and the Cu will be plated on the field region without discrimination. If both field regions and features are exposed simultaneously, then the current would preferentially flow through the features and more Cu would be plated into the features and less on the field regions. This situation can be assured by increasing the number of openings in the mask so that there are always portions of the both regions (field and feature) exposed through some of the holes simultaneously.
If a constant voltage power supply is used, then the current automatically adjusts itself depending upon the resistance on the wafer surface. Therefore, if the mask hole exposes only the field regions of the wafer, less current is supplied to that surface and the plating amount is smaller. When features are exposed to the solution, more current flows into the feature and thus preferential plating takes place into the features. Therefore, it is more appropriate to use a voltage controlled mode of the power supply if wafers with low feature density is coated and/or the number of holes in the mask is limited.
The process described above can be used to fill both small and large features. However, a serial process can also be utilized. In that approach, there are two processing steps. During the first step, the mask is pulled away from the wafer surface, allowing a substantial amount of plating solution between the mask and the wafer surface. In this position, the system acts just like a traditional plating cell. With the help of the additives in the plating solution, the small features are filled during this step and the situation shown in
Along with using copper and its alloys as the conductive material, other conductive materials, such as copper alloys, iron, nickel, chromium, indium, lead, tin, lead-tin alloys, nonleaded solderable alloys, silver, zinc, cadmium, ruthenium, and their respective alloys, may be used. The process is especially suited for the fabrication of high performance and highly reliable chip interconnect, packaging, magnetic, flat panel and opto-electronic applications.
In the previous descriptions, numerous specific details are set forth, such as specific materials, mask designs, pressures, chemicals, processes, etc., to provide a thorough understanding of the embodiments described herein. However, as one having ordinary skill in the art would recognize, the embodiments can be practiced without resorting to the details specifically set forth.
Although various preferred embodiments have been described in detail above, those skilled in the art will readily appreciate that many modifications of the exemplary embodiment are possible without materially departing from the novel teachings and advantages of this invention.
Claims
1. A system for electrodepositing a conductive material onto a surface of a wafer, wherein the surface includes an upper surface portion and a cavity portion, the system comprising:
- an auxiliary chamber configured to have an additive adsorbed on the upper surface portion and the cavity portion of the surface; and
- a plating chamber configured to electrodeposit the conductive material to form a conductive layer on the surface.
2. The system of claim 1, further comprising a workpiece surface influencing device in the plating chamber, the workpiece surface influencing device configured to establish a differential in an adsorbed concentration of the additive between the upper surface portion and the cavity portion of the surface.
3. The system of claim 2, wherein the additive comprises an accelerator.
4. The system of claim 2, wherein the workpiece surface influencing device includes a sweeper.
5. The system of claim 4, wherein the sweeper includes a pad configured to touch the surface of the wafer while the differential is being established.
6. The system of claim 4, further comprising a moving mechanism configured to move the sweeper relative to the surface.
7. The system of claim 1, wherein the auxiliary chamber includes means for applying the additive to the surface of the wafer.
8. The system of claim 7, wherein the means for applying the additive to the surface are nozzles configured to inject the additive towards the surface.
9. The system of claim 7, wherein the additive comprises an accelerator.
10. The system of claim 1, further including a wafer carrier configured to hold the wafer within the auxiliary chamber.
11. The system of claim 1, wherein the plating chamber includes a plating unit with an electrode.
12. The system of claim 11, wherein the plating chamber is configured to supply a plating solution to the plating unit.
13. The system of claim 12, wherein the plating solution includes suppressor additives.
14. The system of claim 1, wherein the conductive material is copper.
15. A system for electrodepositing a conductive material onto a surface of a wafer, wherein the surface includes an upper surface portion and a cavity portion, the system comprising:
- a first chamber including additive applying means for having an additive adsorbed on the upper surface portion and the cavity portion of the surface; and
- a second chamber including a plating means for electrodepositing the conductive material on the surface.
16. The system of claim 15, further comprising an additive differential forming means in the second chamber to establish a differential in an adsorbed concentration of the additive between the upper surface portion and the cavity portion of the surface.
17. The system of claim 15, wherein the additive applying means includes nozzles configured to apply the additive to the surface.
18. The system of claim 16, wherein the additive differential forming means includes a sweeper configured to sweep the surface.
19. The system of claim 15, wherein the plating means includes a deposition unit having an electrode immersed in an electrolyte.
20. The system of claim 19, wherein the electrolyte includes a suppressor.
21. The system of claim 17, wherein the additive comprises an accelerator.
22. The system of claim 18, wherein the sweeper includes a pad configured to touch the surface of the wafer while the differential is being established.
23. The system of claim 18, further comprising a moving mechanism configured to move the sweeper relative to the surface.
24. The system of claim 15, further including a wafer carrier configured to hold the wafer within the first chamber.
25. A method of electrodepositing a conductive material onto a surface of a wafer, wherein the surface includes an upper surface portion and a cavity portion, the method comprising:
- having an additive adsorbed on the surface portion and the cavity portion of the surface in a first chamber;
- transporting the wafer to a second chamber after having the additive adsorbed; and
- electrodepositing the conductive material to form a conductive layer on the surface in the second chamber.
26. The method of claim 25, further comprising establishing a differential in an adsorbed concentration of the additive between the surface portion and the cavity portion of the surface in the second chamber.
27. The method of claim 26, wherein establishing a differential comprises sweeping the surface with a sweeper.
28. The method of claim 27, wherein the additive comprises an accelerator.
29. The method of claim 27, wherein the sweeper includes a pad configured to touch the surface of the wafer while the differential is being established.
30. The method of claim 25, further including applying the additive to the surface of the wafer to have the additive adsorbed on the surface.
31. The method of claim 30, wherein applying comprises injecting the additive towards the surface using nozzles.
32. The method of claim 31, wherein the additive comprises an accelerator.
33. The method of claim 25, further including holding the wafer by a wafer carrier.
34. The method of claim 33, wherein transporting is performed with the wafer carrier.
35. The method of claim 33, wherein transporting is performed with another wafer carrier.
36. The method of claim 25, wherein electrodepositing is performed in the second chamber comprising a plating unit with an electrode and a plating solution.
37. The method of claim 36, wherein the plating solution includes suppressor additives.
38. The method of claim 25, wherein the steps of having the additive adsorbed, transporting the wafer and electrodepositing the conductive material are carried out while the wafer is held by a wafer carrier.
39. The method of claim 25, further including rinsing the wafer after adsorbing the additive and before electrodepositing the conductive material.
40. The method of claim 39, further including drying the wafer after rinsing.
41. The method of claim 25, further including cleaning the wafer after electrodepositing.
42. The method of claim 41, wherein cleaning is carried out in the first chamber.
43. The method of claim 25, wherein the conductive material is copper.
44. A method of electrodepositing a conductive material onto a surface of a wafer, wherein the surface includes a first surface portion and a second surface portion, the method comprising:
- having an additive adsorbed on the first surface portion and the second surface portion of the surface in a first chamber;
- transporting the wafer to a second chamber after having the additive adsorbed; and
- electrodepositing the conductive material to form a conductive layer on the surface in the second chamber using a plating solution while sweeping the first surface portion with a sweeper.
45. The method of claim 44, wherein said sweeping establishes a differential in an adsorbed concentration of the additive between the first surface portion and the second surface portion of the surface.
46. The method of claim 45, wherein the additive comprises an accelerator additive.
47. The method of claim 45, wherein the sweeper includes a pad configured to touch the surface of the wafer while the differential is being established.
48. The method of claim 46, wherein electrodepositing deposits thicker conductive material on the second surface portion than on the first surface portion.
49. The method of claim 48, wherein the plating solution includes a suppressor additive.
50. The method of claim 49, wherein the first surface portion is a top surface portion and the second surface portion is a cavity portion.
Type: Application
Filed: Sep 26, 2005
Publication Date: Apr 20, 2006
Inventor: Bulent Basol (Manhattan Beach, CA)
Application Number: 11/237,991
International Classification: C25D 7/12 (20060101);